XPA-Mediated Regulation of Global Nucleotide Excision Repair by ATR Is p53-Dependent and Occurs Primarily in S-Phase

por Li, Zhengke, Musich, Phillip R., Serrano, Moises A., Dong, Zhiping, Zou, Yue
Publicado 2011

Comparative Benchmarking of Optical Genome Mapping and Chromosomal Microarray Reveals High Technological Concordance in CNV Identification and Additional Structural Variant Refinem...

por Barseghyan, Hayk, Pang, Andy Wing Chun, Clifford, Benjamin, Serrano, Moises A., Chaubey, Alka, Hastie, Alex R.
Publicado 2023

DNA-PK, ATM and ATR collaboratively regulate p53-RPA interaction to facilitate homologous recombination DNA repair

por Serrano, Moises A., Li, Zhengke, Dangeti, Mohan, Musich, Phillip R., Patrick, Steve, Roginskaya, Marina, Cartwright, Brian, Zou, Yue
Publicado 2012

Parent-of-Origin Effects in 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) Syndrome

por Davis, Kyle W., Serrano, Moises, Loddo, Sara, Robinson, Catherine, Alesi, Viola, Dallapiccola, Bruno, Novelli, Antonio, Butler, Merlin G.
Publicado 2019

NeuroSCORE is a genome-wide omics-based model that identifies candidate disease genes of the central nervous system

por Davis, Kyle W., Bilancia, Colleen G., Martin, Megan, Vanzo, Rena, Rimmasch, Megan, Hom, Yolanda, Uddin, Mohammed, Serrano, Moises A.
Publicado 2022

Clinical utility of exome sequencing in individuals with large homozygous regions detected by chromosomal microarray analysis

por Prasad, Aparna, Sdano, Matthew A., Vanzo, Rena J., Mowery-Rushton, Patricia A., Serrano, Moises A., Hensel, Charles H., Wassman, E. Robert
Publicado 2018

The Temple Grandin Genome: Comprehensive Analysis in a Scientist with High-Functioning Autism

por Vanzo, Rena J., Prasad, Aparna, Staunch, Lauren, Hensel, Charles H., Serrano, Moises A., Wassman, E. Robert, Kaplun, Alexander, Grandin, Temple, Boles, Richard G.
Publicado 2020

Clinical Performance of an Ultrahigh Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders

por Ho, Karen S., Twede, Hope, Vanzo, Rena, Harward, Erin, Hensel, Charles H., Martin, Megan M., Page, Stephanie, Peiffer, Andreas, Mowery-Rushton, Patricia, Serrano, Moises, Wassman, E. Robert
Publicado 2016

Analytical and Clinical Validity Study of FirstStepDx PLUS: A Chromosomal Microarray Optimized for Patients with Neurodevelopmental Conditions

por Hensel, Charles, Vanzo, Rena, Martin, Megan, Dixon, Sean, Lambert, Christophe, Levy, Brynn, Nelson, Lesa, Peiffer, Andy, Ho, Karen S., Rushton, Patricia, Serrano, Moises, South, Sarah, Ward, Kenneth, Wassman, Edward
Publicado 2017

Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disorders

por Wassman, E. Robert, Ho, Karen S., Bertrand, Diana, Davis, Kyle W., Martin, Megan M., Page, Stephanie, Peiffer, Andreas, Prasad, Aparna, Serrano, Moises A., Twede, Hope, Vanzo, Rena, Scherer, Stephen W., Uddin, Mohammed, Hensel, Charles H.
Publicado 2019

Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders

por Costain, Gregory, Walker, Susan, Argiropoulos, Bob, Baribeau, Danielle A., Bassett, Anne S., Boot, Erik, Devriendt, Koen, Kellam, Barbara, Marshall, Christian R., Prasad, Aparna, Serrano, Moises A., Stavropoulos, D. James, Twede, Hope, Vermeesch, Joris R., Vorstman, Jacob A. S., Scherer, Stephen W.
Publicado 2019